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1,6:2,3-dianhydro-4-deoxy-β-D-lyxo-hexopyranose is a complex carbohydrate compound derived from the dehydration of a sugar molecule. It is a structurally modified form of a hexose sugar, specifically β-D-lyxo-hexopyranose, with the removal of a hydroxyl group at the 4th carbon and the formation of two anhydro bridges, one between carbons 1 and 6, and another between carbons 2 and 3. This modification results in a more rigid and stable structure compared to the parent sugar. The compound is of interest in the field of organic chemistry and carbohydrate chemistry, as it represents a unique structural variant that can be used in the synthesis of various biologically active compounds and as a building block in the development of new pharmaceuticals and materials.

279-17-4

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279-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 279-17-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 279-17:
(5*2)+(4*7)+(3*9)+(2*1)+(1*7)=74
74 % 10 = 4
So 279-17-4 is a valid CAS Registry Number.

279-17-4Relevant academic research and scientific papers

PREPARATION OF 2-AMINO-2,4-DIDEOXY-D-lyxo-HEXOPYRANOSE (4-DEOXY-D-MANNOSAMINE) FROM 1,6-ANHYDRO-β-D-GLUCOPYRANOSE

Cerny, Ivan,Trnka, Tomas,Cerny, Miloslav

, p. 2386 - 2394 (2007/10/02)

1,6-Anhydro-4-deoxy-2-O-p-toluenesulfonyl-β-D-xylo-hexopyranose (III), obtainable by a four-step synthesis from 1,6-anhydro-β-D-glucopyranose, was converted to 3-O-(N-benzylcarbamoyl) derivative V on reaction with benzyl isocyanate.The cyclization of V wi

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